Users can query the SNP information according to the gene ID.


Gene ID

Results: 1 - 489298 of 489298 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
13251 BAA01g10410 A01 4760135 G A upstream_gene_variant MODIFIER c.-2932C>T| S244
S263
13252 BAA01g10410 A01 4760612 G A upstream_gene_variant MODIFIER c.-3409C>T| S95
13253 BAA01g10410 A01 4760648 G A upstream_gene_variant MODIFIER c.-3445C>T| S15
13254 BAA01g10410 A01 4761112 C T upstream_gene_variant MODIFIER c.-3909G>A| S48
13255 BAA01g10410 A01 4761938 C T upstream_gene_variant MODIFIER c.-4735G>A| S150
13256 BAA01g10410 A01 4762110 C T upstream_gene_variant MODIFIER c.-4907G>A| S16
13257 BAA01g10410 A01 4762199 G A upstream_gene_variant MODIFIER c.-4996C>T| S293
13258 BAA01g10420 A01 4762433 C T downstream_gene_variant MODIFIER c.*1527C>T| S305
13259 BAA01g10420 A01 4764280 C T downstream_gene_variant MODIFIER c.*3374C>T| S61
13260 BAA01g10420 A01 4764547 G A downstream_gene_variant MODIFIER c.*3641G>A| S204
13261 BAA01g10420 A01 4764565 C T downstream_gene_variant MODIFIER c.*3659C>T| S265
13262 BAA01g10430 A01 4766203 C T missense_variant MODERATE c.265G>A|p.Gly89Arg S203
13263 BAA01g10430 A01 4768652 C T upstream_gene_variant MODIFIER c.-2073G>A| S249
13264 BAA01g10430 A01 4770671 C T upstream_gene_variant MODIFIER c.-4092G>A| S192
13265 BAA01g10430 A01 4771019 G A upstream_gene_variant MODIFIER c.-4440C>T| S33
13266 BAA01g10440 A01 4773877 G A downstream_gene_variant MODIFIER c.*2116C>T| S204
13267 BAA01g10440 A01 4774063 C T downstream_gene_variant MODIFIER c.*1930G>A| S125
13268 BAA01g10440 A01 4774761 C T downstream_gene_variant MODIFIER c.*1232G>A| S158
13269 BAA01g10440 A01 4774986 C T downstream_gene_variant MODIFIER c.*1007G>A| S249
13270 BAA01g10440 A01 4775452 G A downstream_gene_variant MODIFIER c.*541C>T| S56
13271 BAA01g10440 A01 4775460 C T downstream_gene_variant MODIFIER c.*533G>A| S45
13272 BAA01g10440 A01 4775687 G A downstream_gene_variant MODIFIER c.*306C>T| S247
13273 BAA01g10440 A01 4776384 C T missense_variant MODERATE c.1171G>A|p.Gly391Arg S170
13274 BAA01g10440 A01 4777470 G A intron_variant MODIFIER c.439+22C>T| S8
13275 BAA01g10440 A01 4778473 G A intron_variant MODIFIER c.76+29C>T| S191